BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    PERCUTANEOUS INTRODUCER COURNAND STYLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ERA® Implant Abutment Micro Ang. Base, 2.25mm Cuff (AE)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549106354·Implant retained overdentures are an establishe...

    ISPVAC TM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DigitalDiagnost C90

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIFEVEST WCD 4000 SYS

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·April 25, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    REPAIR CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·August 11, 2010